These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 6224733)

  • 1. Origin of chromosomal abnormalities: evidence for delayed fertilization in meiotic nondisjunction.
    Juberg RC
    Hum Genet; 1983; 64(2):122-7. PubMed ID: 6224733
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nondisjunction in trisomy 21: origin and mechanisms.
    Petersen MB; Mikkelsen M
    Cytogenet Cell Genet; 2000; 91(1-4):199-203. PubMed ID: 11173856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Issues pertaining to the impact and etiology of trisomy 21 and other aneuploidy in humans; a consideration of evolutionary implications, maternal age mechanisms, and other matters.
    Hook EB
    Prog Clin Biol Res; 1989; 311():1-27. PubMed ID: 2528149
    [No Abstract]   [Full Text] [Related]  

  • 4. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
    Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clustering of chromosomal aneuploidy and tracing of nondisjunction in man.
    Hansmann I
    Environ Health Perspect; 1979 Aug; 31():23-5. PubMed ID: 159172
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data.
    Ghosh S; Bhaumik P; Ghosh P; Dey SK
    Genet Res (Camb); 2010 Jun; 92(3):189-97. PubMed ID: 20667163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Acrocentric chromosomal associations in the families of children with Down's disease].
    Kovaleva NV; Butomo IV; Novikova IIu
    Tsitologiia; 1993; 35(10):33-43. PubMed ID: 8165746
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sperm aging in the male and cytogenetic anomalies. An animal model.
    Martin-DeLeon PA; Boice ML
    Hum Genet; 1982; 62(1):70-7. PubMed ID: 6218064
    [No Abstract]   [Full Text] [Related]  

  • 9. Chromosomal differences in susceptibility to meiotic aneuploidy.
    Warburton D; Kinney A
    Environ Mol Mutagen; 1996; 28(3):237-47. PubMed ID: 8908182
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects.
    Zittergruen MM; Murray JC; Lauer RM; Burns TL; Sheffield VC
    Circulation; 1995 Nov; 92(10):2803-10. PubMed ID: 7586245
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [The parental origin of the extra chromosome 21 in Down's syndrome].
    Hamers AJ; Heijnen GC; Jongbloet PH
    Tijdschr Kindergeneeskd; 1983 Oct; 51(5):157-62. PubMed ID: 6230758
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
    Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
    Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Paternal nondisjunction in trisomy 21: excess of male patients.
    Petersen MB; Antonarakis SE; Hassold TJ; Freeman SB; Sherman SL; Avramopoulos D; Mikkelsen M
    Hum Mol Genet; 1993 Oct; 2(10):1691-5. PubMed ID: 8268923
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy in man.
    Hassold TJ; Jacobs PA
    Annu Rev Genet; 1984; 18():69-97. PubMed ID: 6241455
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
    Ballesta F; Queralt R; Gómez D; Solsona E; Guitart M; Ezquerra M; Moreno J; Oliva R
    Ann Genet; 1999; 42(1):11-5. PubMed ID: 10214502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequence of centromere separation another mechanism for the origin of nondisjunction.
    Vig BK
    Hum Genet; 1984; 66(2-3):239-43. PubMed ID: 6232200
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parental origin of chromosome abnormalities in spontaneous abortions.
    Meulenbroek GH; Geraedts JP
    Hum Genet; 1982; 62(2):129-33. PubMed ID: 7160845
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Parental age and the origin of trisomy 21. A study of 302 families.
    Dagna Bricarelli F; Pierluigi M; Landucci M; Arslanian A; Coviello DA; Ferro MA; Strigini P
    Hum Genet; 1989 Apr; 82(1):20-6. PubMed ID: 2523851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Chromosome abnormalities of human gametes].
    Sèle B; Pellestor F; Rousseaux S; Raymond L; Cozzi J; Pelletier R
    Reprod Nutr Dev; 1990; Suppl 1():75s-82s. PubMed ID: 2206295
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The associations of acrocentric chromosomes in the parents of Down's syndrome children (a review of the literature)].
    Kovaleva NV
    Tsitologiia; 1991; 33(6):3-11. PubMed ID: 1840366
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.